Better quality of response to lenalidomide plus dexamethasone is associated with improved clinical outcomes in patients with relapsed or refractory multiple myeloma

被引:93
作者
Harousseau, Jean-Luc [1 ]
Dimopoulos, Meletios A. [2 ]
Wang, Michael [3 ]
Corso, Alessandro [4 ]
Chen, Christine [5 ]
Attal, Michel [6 ]
Spencer, Andrew [7 ]
Yu, Zhinuan [8 ]
Olesnyckyj, Marta [8 ]
Zeldis, Jerome B. [8 ]
Knight, Robert D. [8 ]
Weber, Donna M. [3 ]
机构
[1] Ctr Rene Gauducheau, F-44805 Nantes, St Herblain, France
[2] Univ Athens, Sch Med, Dept Clin Therapeut, GR-11527 Athens, Greece
[3] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[4] Univ Pavia, Fdn IRCCS Policlin S Matteo, Div Hematol, I-27100 Pavia, Italy
[5] Princess Margaret Hosp, Toronto, ON M4X 1K9, Canada
[6] CHU Purpan, Div Hematol, Toulouse, France
[7] Alfred Hosp, Melbourne, Vic, Australia
[8] Celgene Corp, Summit, NJ USA
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2010年 / 95卷 / 10期
关键词
lenalidomide; dexamethasone; multiple myeloma; response; clinical benefit; efficacy; FOLLOW-UP; PHASE-I; BORTEZOMIB; THERAPY; TRIAL; COMBINATION; SURVIVAL; TRANSPLANTATION; EFFICACY; SAFETY;
D O I
10.3324/haematol.2009.015917
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background This retrospective pooled analysis of two phase III trials (MM-009/MM-010) compared clinical outcomes of patients who achieved a complete response or very good partial response to treatment with lenalidomide plus dexamethasone with the outcomes of those who only achieved a partial response. Design and Methods Patients (n=353) received lenalidomide (25 mg/day for 21 days of each 28-day cycle) plus dexamethasone (40 mg on days 1-4, 9-12, and 17-20 for four cycles, and only on days 1-4 after the first four cycles). Time to response, duration of response, time-to-progression, overall survival, and adverse events were investigated for patients who had a complete or very good partial response and compared with those of patients who had a partial response. Results At the time of unblinding, 32% of patients had achieved a complete or very good partial response and 28% had a partial response. Half (50.5%) of the patients who had a partial response as their initial response achieved a complete or very good partial response with further treatment. The probability of achieving a complete or very good partial response with continued lenalidomide treatment decreased with delayed achievement of a partial response (by cycle 4 versus later); however, it remained clinically significant. With an extended follow-up of 48 months, the median response duration, time-to-progression, and overall survival were longer in patients with a complete or very good partial response than in those with a partial response (24.0 versus 8.3 months, P<0.001; 27.7 versus 12.0 months, P<0.001; not reached versus 44.2 months, P=0.021, respectively). The benefit of a complete or very good partial response was independent of when it was achieved. Conclusions Continuing treatment with lenalidomide plus dexamethasone to achieve best response, in the absence of disease progression and toxicity, provided deeper remissions and greater clinical benefit over time for patients in this study.
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收藏
页码:1738 / 1744
页数:7
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